School of Pharmacy, Binzhou Medical University, Yantai 264003, Shandong Province, China.
Shandong Technology Innovation Center of Molecular Targeting and Intelligent Diagnosis and Treatment, Yantai 264003, Shandong Province, China.
J Neurosci. 2024 Jun 26;44(26):e0252242024. doi: 10.1523/JNEUROSCI.0252-24.2024.
The striatum plays a central role in directing many complex behaviors ranging from motor control to action choice and reward learning. In our study, we used 55 male CFW mice with rapid decay linkage disequilibrium to systematically mine the striatum-related behavioral functional genes by analyzing their striatal transcriptomes and 79 measured behavioral phenotypic data. By constructing a gene coexpression network, we clustered the genes into 13 modules, with most of them being positively correlated with motor traits. Based on functional annotations as well as Fisher's exact and hypergeometric distribution tests, brown and magenta modules were identified as core modules. They were significantly enriched for striatal-related functional genes. Subsequent Mendelian randomization analysis verified the causal relationship between the core modules and dyskinesia. Through the intramodular gene connectivity analysis, and were identified as brown and magenta module hub genes, respectively. Knock outs of both and lead to motor dysfunction in mice, and acts as a risk gene for schizophrenia and smoking addiction in humans. We also evaluated the cellular composition of each module and identified oligodendrocytes in the striatum to have a positive role in motor regulation.
纹状体在指导许多复杂行为方面起着核心作用,这些行为从运动控制到动作选择和奖励学习不等。在我们的研究中,我们使用了 55 只具有快速衰减连锁不平衡的雄性 CFW 小鼠,通过分析它们的纹状体转录组和 79 个测量的行为表型数据,系统地挖掘纹状体相关的行为功能基因。通过构建基因共表达网络,我们将基因聚类为 13 个模块,其中大多数与运动特征呈正相关。基于功能注释以及 Fisher 精确检验和超几何分布检验,棕色和品红色模块被鉴定为核心模块。它们显著富集了与纹状体相关的功能基因。随后的孟德尔随机化分析验证了核心模块与运动障碍之间的因果关系。通过模块内基因连接性分析,分别鉴定出 和 为棕色和品红色模块的枢纽基因。敲除 和 都会导致小鼠运动功能障碍,而 在人类中是精神分裂症和吸烟成瘾的风险基因。我们还评估了每个模块的细胞组成,并确定了纹状体中的少突胶质细胞在运动调节中具有积极作用。